Developmental syndromes and malformations of the urinary tract

بواسطة Chanin Limwongse
منشور في 2018

Liddle’s syndrome: A case report

بواسطة Meta Phoojaroenchanachai, Peera Buranakitjaroen, Chanin Limwongse
منشور في 2018

Real-time three dimensional sonographic features of an early third trimester fetus with achondrogenesis

بواسطة Tuangsit Wataganara, Anuwat Sutanthavibool, Chanin Limwongse
منشور في 2018

Incidence and risk factors of vascular dementia in Thai stroke patients

بواسطة Pornpatr A. Dharmasaroja, Chanin Limwongse, Thammanard Charernboon
منشور في 2020

A novel mutation in the β-subunit of the epithelial sodium channel gene (SCNN1B) in a Thai family with Liddle's syndrome

بواسطة Pairunyar Sawathiparnich, Achra Sumboonnanonda, Praewvarin Weerakulwattana, Chanin Limwongse
منشور في 2018

Ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome presenting with a large nephrogenic cyst, severe oligohydramnios and hydrops fetalis: A case report and review of the lite...

بواسطة Tuenjai Chuangsuwanich, Prasert Sunsaneevithayakul, Kobkun Muangsomboon, Chanin Limwongse
منشور في 2018

Polyglutamined expanded androgen receptor interacts with chaperonin CCT

بواسطة Suttikarn Pongtepaditep, Thawornchai Limjindaporn, Patcharee Lertrit, Chatchawan Srisawat, Chanin Limwongse
منشور في 2018

Influence of CYP2D6, CYP3A5, ABCB1, APOE polymorphisms and nongenetic factors on donepezil treatment in patients with Alzheimer’s disease and vascular dementia

بواسطة Thitipon Yaowaluk, Vorapun Senanarong, Chanin Limwongse, Rasda Boonprasert, Pornpimol Kijsanayotin
منشور في 2020

Autosomal recessive spastic ataxia of charlevoixsaguenay (Arsacs) in a thai patient: The classic clinical manifestations, funduscopic feature, and brain imaging findings with a nov...

بواسطة Jindapa Srikajon, Yuvadee Pitakpatapee, Chanin Limwongse, Niphon Chirapapaisan, Prachaya Srivanitchapoom
منشور في 2020

A Thai family with hereditary pancreatitis and increased cancer risk due to a mutation in PRSS1 gene

بواسطة Theeraphong Pho-Iam, Wanna Thongnoppakhun, Pai Thai Yenchitsomanus, Chanin Limwongse
منشور في 2018

Contribution to decreased susceptibility to liver cancer in thais

بواسطة Chonlada Viratroumanee, Pornpen Pramyothin, Chanin Limwongse, Payiarat Suwannasri, Anunchai Assawamakin
منشور في 2018

Glutathione S-transferase polymorphisms and risk of bladder cancer in Thais

بواسطة Kannika Pradubkaew, Pornpen Pramyothin, Chanin Limwongse, Payiarat Suwannasri, Anunchai Assawamakin
منشور في 2018

Combination of multiplex PCR and DHPLC-based strategy for CYP2D6 genotyping scheme in Thais

بواسطة Payiarat Suwannasri, Wanna Thongnoppakhun, Pornpen Pramyothin, Anunchai Assawamakin, Chanin Limwongse
منشور في 2018

Floppy infant caused by MTM1 mutation: A first genetically-confirmed X-linked myotubular myopathy patient in Thailand

بواسطة Teerin Liewluck, Natte Raksadawan, Chanin Limwongse, Ichizo Nishino, Tumtip Sangruchi
منشور في 2018

Severe plexiform facial neurofibromatosis, type 1 with underdeveloped eyes and a novel NF1 mutation

بواسطة Piranit Nik Kantaputra, Ans van den Ouweland, Tumtip Sangruchi, Chanin Limwongse
منشور في 2018

A newly recognized polyosteolysis/hyperostosis syndrome

بواسطة Piranit N. Kantaputra, Chanin Limwongse, Ajchara Koolvisoot, Apichart Ausawamongkolkul, Somsiri Tayavitit
منشور في 2018

Mutations of AML1 in non-MO acute myeloid leukemia: Six novel mutations and a high incidence of cooperative events in a South-east Asian population

بواسطة Chirayu U. Auewarakul, Amporn Leecharendkeat, Wanna Thongnoppakhun, Chanin Limwongse, Chintana Tocharoentanaphol
منشور في 2018

Severe plexiform facial neurofibromatosis, type 1 with underdeveloped eyes and a novel NF1 mutation

بواسطة Piranit Nik Kantaputra, Ans van den Ouweland, Tumtip Sangruchi, Chanin Limwongse
منشور في 2018

Sleep Disorder: An Overlooked Manifestation of Glucose Transporter Type-1 Deficiency Syndrome

بواسطة Kingthong Anurat, Chaiyos Khongkhatithum, Thipwimol Tim-Aroon, Chanin Limwongse, Lunliya Thampratankul
منشور في 2022

Genotype and age at diagnosis in Thai boys with Duchenne muscular dystrophy (DMD)

بواسطة Pattareeya Yamputchong, Theeraphong Pho-iam, Chanin Limwongse, Duangrurdee Wattanasirichaigoon, Oranee Sanmaneechai
منشور في 2020